Kite Pharma receives FDA breakthrough therapy designation for KTE-C19
KTE-C19 is an investigational therapy in which a patient’s T cells are genetically modified to express a chimeric antigen receptor designed to target the antigen CD19, a protein
Teijin Pharma has signed a joint research agreement with Tokyo-based Aska Pharmaceutical to develop small-molecule drug candidates for gynaecological diseases.
The financing, which was supported by institutional investors in the US and Europe, will support the continued clinical development of the company’s ERY-ASP/GRASPA. ERY-ASP/GRASPA is designed specifically to
The program is part of a collaboration between AstraZeneca and its worldwide biologics research and development unit MedImmune. It is intended at developing and commercializing durvalumab across various
Bial director of research & development department Patrício Soares-da-Silva said: "The study met its primary endpoint, which was the proportion of seizure-free patients for six consecutive months under
ADCT plans to initiate Phase I clinical trials in both NHL and ALL. ADCT-402 combines a humanized monoclonal antibody targeting CD19 with a pyrrolobenzodiazepine (PBD) warhead. In preclinical